A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279899



Internal ID20846939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125667335..125669180hg38UCSC Ensembl
chr9:128429614..128431459hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381846
hg191846
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569378
Supporting Variants
Samples
Known GenesMAPKAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279899
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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